Current medical capabilities are one of the foundations of our modern standard of living. Improved techniques and equipment, combined with a deep understanding of the field, have made routine procedures possible that seemed impossible just a few decades ago. These new capabilities have also led to an increase in the number of procedures performed. Nevertheless, every medical procedure carries a risk – among other things, due to the introduction of foreign substances into the body. For this reason, too, the issue of "cleanliness" is a particular focus in the field of medical devices.
The seminar will present typical tests for biological, chemical and particulate contamination in detail and explain their relevance in the context of cleaning validation.
The theoretical part will be followed by a tour of the laboratory.
Overview of topics
- Typical tests within the scope of cleaning validation
- Typical test packages within the scope of cleaning validation
- Approaches to investigating the causes of poor results
Target group
Employees from the medical device manufacturing sector, QM managers and regulatory affairs specialists.
Prior knowledge
None required.
Register here